Tag | Content |
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EnhancerAtlas ID | HS052-07169 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr11:74741120-74743290 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr11:74743197-74743216 | CCGCGCCCCCTGCTGGTTC | - | 6.25 | Gata4 | MA0482.1 | chr11:74742584-74742595 | TCTTATCTCTT | + | 6.02 | Nr5a2 | MA0505.1 | chr11:74742909-74742924 | GGTGACCTTGACCTC | - | 7.13 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I075029 | chr11 | 74740740 | 74743761 |
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Enhancer Sequence | TCTCATCTTC CTGCTTAGGA TTCTCCTCTA CACATGCCAT TTTGCCCCAG TGGAGAACAG 60 GAGTGCAGGG TTAGTGGGTT GGGGGTGGGG GACCTCCCCA TGTGAGGGCA GCAGGCAACC 120 TGAGGACATC CCACACTGCA TTTCAGTGCT GCATCTGCTA CACTGGGGAA GGATAAAATT 180 ATCCACTGCC CACGTCATGT ATCTCCCCAT CCGACGGGGA CTAGAGATAA AAAATGAATG 240 ACACAAAATC CAATCTTGCC TGGTGCAGAA GCTGGTGGGG GTGGGGGTGG AGCTGGTGGC 300 CCAAGCAGCC ACTCATTGCA CAGCACATCT CATATTTATT GACTCATAAT TGAAGGCAGC 360 CTGGAGATGT CCCAGCATTG GCCCCTGACA AGACAGATGA GGGCAAAATG ACTGTGGAGG 420 CAGAGAGTCA GGATACAGAC TTCCTCACAG GACTGCAGCC ACAGAAGGGA GGCAATGGTG 480 GGGAGTGGGG ACAGCTAACT GGCTGTTGCA CTGGCCCCGG GGTCTGACTC GGGTTCTAGG 540 TCCTGCTCTG CTACCCACTT GTGATTACCT TGAACCAGAC CCTCCCCTCT CTAGGCCAGT 600 AATTTTAGCC TTCTTGATTT CATTACCAGG GTTTAGGAAA ATCATTCTGG GAGTTGGGAA 660 AATCTGGGCT GCTAACTTGC TCTGTGGCTT TAGGTGAGTT TCTTTACTCT AAGGGCTTTG 720 TGCTTTCTCT TTGTAAAGAG GAAAGGATGC CTCCCTCTTC TATATAAAGA TTGAGGGGGT 780 TGGGTTGGCC TAGGAGCAGC CAGTTTGTGC ATTTTAGCAA CTGGAAAGCT TCTGGTTGGG 840 GGAAGACAAA GAAACAAGAA ATGCTGCCAA ATATTAAGAA CCTGCAATGA CTCCTAATTG 900 CTCACAGAAA TGGTCCAAAT TCCTAGGCTT GGCATTCAAG GCTGTGAAAC CTGCATAGTC 960 CTACCTCTAG TATTTGTGTC ATTATGGGGA AAGTGTCTGG GGCTGGCAGC CAGGAAGCCT 1020 GGGTTCTGGA CCAGTCTTAC CACTATCTAG CTCTGTGATC TCTGGCAAGT TCTTGATCAT 1080 CTCCAGGTCT CAGTTTCCCC ATCTGTAAAA TTTACATAGG TGATCTATGA AGTAATTAGG 1140 GTCCCCAAGC CCAGAGCAAG TCAGTTGCCA AGTTCTATCC TCTCTCCCTC TCAGTATTCC 1200 CTAAATCCAT TCCTCCCTCA CCCCCATTCC ATTCTAATTA TGACCACTGT CTCACCTCAG 1260 TACTCCTTTC TCTCTTCCTG ACCAGTGCAG TAGCCTCTTG TCTCCCAGCC TCCATCTACC 1320 CCCTCCATAC TCCAGTCAGA GTGACTCAGA AAGCATGTGA CTGACCATGA CCCTCGCCTG 1380 CGTCAAGCCC TTCCTGTGCT CTCCACACAG CTCTCAGCCG AGCTCCTGAG TGTCACATGG 1440 AAGATCCTGC ATGATCTGGC CCTATCTTAT CTCTTTTCCC ACTCCTCCTG TGCCCCGACT 1500 ATCTGTACCA TTCAGGCTGG CCTCTTCACT GCCCTCTCTC CAGCTCAGAC TCCAGGATGA 1560 GGCTTCCCCA AGCTGGCCAG GAGGAGGCCC TGTGGCCCTG AACACAGTAG TAGGTGGGGT 1620 CAGTGTCATG CCTAGACTCC TGTTCTGCCT TTCCAGAAGC TTCTGGAGTT CCAAGCCCCA 1680 TAGGGGTCCT GCTCCATGGA GTCCCCAGAG CATCAGGTGT GAATGATGCT GCCTGTTCTC 1740 CCTCCTGCTG CTGACAACCA GAGAATGTCT GAGCCAAAAG GGCCCCAGAG GTGACCTTGA 1800 CCTCCTAAAA CCCCACATTG TATAGATGGA GAAACTGAGG CCCAGGGAGG AGCAGTGGTC 1860 ACACAGCAAG TCAGTGTTCA TCAGGGCTGG AGCTCTGCCT TGTGCCTGCT CCATGGGGTT 1920 GGGGACACAG GGCTGGACTA GGGTAGCCAT AAAGAGAACA CTCCACGCAC TGGGGCAGGA 1980 GGGGCCATCA GCCCTCCCTT CAGTGGTGGA GGTGAGATAC TCAGCAGGAG ACTCAGGGCA 2040 GGGAAAGAGG CTTCTGCCAG TCTCATTCCC ATCCTCACCG CGCCCCCTGC TGGTTCTGTC 2100 CTATTAGGGC TTCCAGGTCT CTGTACTTTA CCTCCTCGCC ACATGTCCAG CCTTCCTGAG 2160 GTGGGATGGG 2170
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